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U.S. Department of Health and Human Services

510(k) Premarket Notification

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Device Classification Name powered laser surgical instrument
510(k) Number K902940
Device Name CARDIOLASE YAG MODEL 4000 SURGICAL LASER SYSTEM
Original Applicant
TRIMEDYNE, INC.
1311 valencia ave.
tustin,  CA  92680
Original Contact merritt m girgis
Regulation Number878.4810
Classification Product Code
GEX  
Date Received07/03/1990
Decision Date 10/03/1990
Decision substantially equivalent (SESE)
Regulation Medical Specialty General & Plastic Surgery
510k Review Panel General & Plastic Surgery
Type Traditional
Reviewed by Third Party No
Combination Product No
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